Sentence examples for criterion of toxicity from inspiring English sources

Criterion of toxicity for fractions was categorized as nontoxic (LC50 values > 1000  μg/mL), poor toxic (500 1000  μg/mL), and toxic (<500  μg/mL) according to Déciga-Campos et al. [ 43].

Thus, it is inappropriate to use a fixed criterion of toxicity for categorization, such as the 10 μg/L recommended in Regulation 1107/2009 [10] as this will lead to false negatives and false positives.

Criterion of toxicity for fractions was established according to Déciga-campos et al. [ 23]: LC50 values > 1000 μg/mL (non-toxic), ≥ 500 ≤ 1000 μg/mL (weak toxicity) and < 500 μg/mL (toxic).

Nonetheless, one question remains unanswered; it is not yet known which of the three drugs approved in second-line treatment should be selected, unless the criterion of toxicity profile is applied.

Concentrations in aquatic systems in the USA have been thoroughly reviewed [25] and were not included in the assessment presented here other than in the context of assessing exceedences of criteria for toxicity and their rapid response to changes in pattern of use.

The accuracy of the model was assessed in terms of three criteria: nadir timing (criterion i), neutrophil counts (criterion ii) and grade of toxicity per cycle (criterion iii).

The criterion for toxicity for classification of POPs is 'significant adverse effects' without a clear definition of 'significant' or the location of the effects.

Since pesticides are designed to be toxic to at least some groups of organisms, the criterion for assessment of toxicity is likely to capture all pesticides.

The criteria for toxicity of terrestrial organisms are not provided either in Regulation 1107/2009 [10] or the REACH Regulation 253/2011 [5].

In our study, only 29% of the patients developed thrombocytopenia in the first treatment cycle as compared with 46% of the patients who developed leukopenia scored according to the criteria of Common Toxicity Criteria for Adverse Events version 3.0.

Based on independently reviewed imaging, the primary end point of time-to-progression had exceeded the predetermined stopping criteria, and review of toxicity data indicated no substantive safety concerns.